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rs377025174

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377025174(C;T)
Make rs377025174(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position218661192
GeneBCS1L, ZNF142
is asnp
is mentioned by
dbSNPrs377025174
ebirs377025174
HLIrs377025174
Exacrs377025174
Varsomers377025174
Maprs377025174
PheGenIrs377025174
hapmaprs377025174
1000 genomesrs377025174
hgdprs377025174
ensemblrs377025174
gopubmedrs377025174
geneviewrs377025174
scholarrs377025174
googlers377025174
pharmgkbrs377025174
gwascentralrs377025174
openSNPrs377025174
23andMers377025174
23andMe allrs377025174
SNP Nexus

SNPshotrs377025174
SNPdbers377025174
MSV3drs377025174
GWAS Ctlgrs377025174
Max Magnitude0
ClinVar
Risk rs377025174(T;T)
Alt rs377025174(T;T)
Reference rs377025174(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BCS1L ZNF142
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.219525915C>T
CLNSRC
CLNACC RCV000197059.2,